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Standard

Serum alkaline phosphatase levels

FUT1 · rs4021

Strength of the evidence

3 / 4

Its strongest genetic-study result is p = 10−124, with 21 associations in the GWAS Catalog.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What the study found

Who was studied 342,535 European ancestry individuals, 6,019 African ancestry individuals, 7,337 South Asian ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0627 higher (95% confidence interval 0.058-0.068); p = 2 × 10−124.

Where it sits Chromosome 19, band 19q13.33 — in the 3′ untranslated region of FUT1.

How common each version is

AG
Korean KRGDB
A 67.3% · G 32.7%
Korean Korea4K
A 68.3% · G 31.7%
Korean Korea1K
A 67.6% · G 32.4%
Japanese ToMMo
A 66.0% · G 34.0%
Vietnamese
A 44.4% · G 55.6%
World gnomAD
A 61.5% · G 38.5%
World 1000 Genomes
A 55.6% · G 44.4%
World TOPMed
A 60.3% · G 39.7%

The share of all copies of this position that are each version. Source: the population studies published in dbSNP (US NCBI); each row names its study.

What each result means

A/A No copy of the version the research linked to Serum alkaline phosphatase levels. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Serum alkaline phosphatase levels. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Serum alkaline phosphatase levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Quoting this page

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Serum alkaline phosphatase levels (rs4021). MyGeneLog™. https://www.mygenelog.com/variants/rs4021

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